Stability and reactivity of grafted Cr(CO)3 species on MOF linkers: a computational study.

Inorg Chem

Dipartimento di Chimica IFM and NIS Centre of Excellence, Università di Torino, Via Pietro Giuria 7, 10125 Torino, Italia.

Published: June 2009

The possibility to modulate Cr(CO)(3) properties by grafting it onto metal-organic framework (MOF) linkers of different natures has been investigated using density functional methods. MOF linkers were modeled using clusters constituted by benzene rings doubly substituted in the para position. The effect of the electron-donor or electron-acceptor nature of benzene substituents on the stability of the (eta(6)-arene)Cr(CO)(3) adduct and on the shift of the CO bands has been considered. Different electron-donor (-NH(2), -CH(3), -OH, -COONa) and electron-acceptor (-F, -COOH, -CN, -CF(3)) substituents have been used and the results compared with the bare benzene. C(6)H(4)(COOZnOH)(2) and C(6)H(4)(Zn(4)O(13)C(6)H(5))(2) clusters have also been adopted as models of the MOF-5 benzene rings. The possibility of modulating the stability and the reactivity of Cr(CO)(3) species by grafting them to MOFs with different organic linkers was verified. In particular, this study indicates that electron-acceptor (e.g., C(6)H(4)(COOH)(2)) substituted MOF linkers facilitate the substitution of CO by incoming molecules, whereas the use of electron-donor ones (e.g., C(6)H(4)(OH)(2)) would improve the stability of the Cr(CO)(3) adduct and the ring acidity. Furthermore, an almost linear dependence of the Cr(CO)(3) binding energies on the calculated structural and vibrational features of the tricarbonyl was found, suggesting that the stability of the Cr(CO)(3) adduct can be inferred experimentally from vibrational and diffraction data. In the end, on the basis of the results obtained, it was possible to successfully explain the experimental shift of the CO IR stretching features of grafted Cr(CO)(3) on the UiO-66, CPO-27-Ni, and MOF-5 aromatic linkers and on the benzene rings of poly(ethylstyrene-co-divinylbenzene). The sign of the Delta nu(CO) shift with respect to C(6)H(6)Cr(CO)(3) has been found to be strongly dependent on higher/lower electron density on the ring.

Download full-text PDF

Source
http://dx.doi.org/10.1021/ic9004664DOI Listing

Publication Analysis

Top Keywords

mof linkers
16
benzene rings
12
stability reactivity
8
grafted crco3
8
crco3 species
8
stability crco3
8
crco3 adduct
8
crco3
7
linkers
6
stability
5

Similar Publications

Conformation Regulation of Perylene Diimide Derivatives by Lanthanide Coordination for Turn-On Fluorescence Sensing of Sarin Simulants.

Inorg Chem

January 2025

Key Laboratory of Applied Surface and Colloid Chemistry (MOE), School of Chemistry & Chemical Engineering, Shaanxi Normal University, Xi'an, Shaanxi 710062, China.

Fluorescent metal-organic frameworks (MOFs) are promising sensing materials that have received much attention in recent years, in which the organic ligand conformation changes usually lead to variations of their sensing behavior. Based on this, in the present work, perylene diimide (PDI) derivatives with excellent photochemical properties closely related to their conformation and molecule packing fashion were selected as organic linkers to detect sarin simulant diethyl chlorophosphate (DCP). By the coordination interactions with large lanthanide cations through terminal carboxylate groups from the PDI derivative, a series of one-dimensional coordination polymers, named [Ln(PDICl-2COO)(μ-O)(DMF)] (SNNU-112, Ln = Yb/Tb/Sm/Nd/Pr/Gd/Eu/Er/Ce, PDICl-2COOH = ,'-bis(4-benzoic acid)-1,2,6,7-tetrachlorohydrazone-3,4,9,10-tetracarboxylic acid diimide) were synthesized.

View Article and Find Full Text PDF

Immobilizing organic chromophores within the rigid framework of metal-organic frameworks (MOFs) augments fluorescence by effectively curtailing molecular motions. Yet, the substantial interspaces and free volumes inherent to MOFs can undermine photoluminescence efficiency, as they partially constrain intramolecular dynamics. In this study, we achieved optimization of both one- and two-photon excited fluorescence by incorporating linkers into an interpenetrated tetraphenylethene-based MOF (TPE-MOF).

View Article and Find Full Text PDF

The application of temperature-compensated photonic device is hampered by poor accuracy and overly simplistic functions of propagation in photonic integrated circuits (PICs) field. Herein, we report a new library of donor-acceptor metal-organic framework (D-A MOF) with thermally activated delayed fluorescence (TADF) and the fabricating of temperature-compensated photonic device by virtue of the unique temperature response character of TADF emitters. Highly tunable through-space charge transfer (TSCT) of TADF was realized within the D-A MOFs through a novel strategy that synergistically combines the internal heavy atom effect (HAE) with an external HAE, induced by the incorporation of heavy atoms into different components, achieving the regulable photophysical indicators including adjustable PL wavelength (534 to 592 nm) and surging quantum yield (5.

View Article and Find Full Text PDF

New Insights on Iron-Trimesate MOFs for Inorganic As(III) and As(V) Adsorption from Aqueous Media.

Nanomaterials (Basel)

December 2024

Unidad Departamental de Química Analítica, Departamento de Química, Facultad de Ciencias, Universidad de La Laguna, Avda. Astrofísico Fco. Sánchez, s/n, 38206 La Laguna, Spain.

Arsenic contamination of water endangers the health of millions of people worldwide, affecting certain countries and regions with especial severity. Interest in the use of Fe-based metal organic frameworks (MOFs) to remove inorganic arsenic species has increased due to their stability and adsorptive properties. In this study, the performance of a synthesized Nano-{Fe-BTC} MOF, containing iron oxide octahedral chains connected by trimesic acid linkers, in adsorbing As(III) and As(V) species was investigated and compared with commercial BasoliteF300 MOF.

View Article and Find Full Text PDF

Magnetocaloric Effect in 3D Gd(III)-Oxalate Coordination Framework.

Nanomaterials (Basel)

December 2024

Key Laboratory of Structure and Functional Regulation of Hybrid Materials of Ministry of Education, School of Materials Science and Engineering, Institutes of Physical Science and Information Technology, Anhui University, Hefei 230601, China.

Cryogenic magnetic refrigerants based on the magnetocaloric effect (MCE) hold significant potential as substitutes for the expensive and scarce He-3. Gd(III)-based complexes are considered excellent candidates for low-temperature magnetic refrigerants. We have synthesized a series of Ln(III)-based metal-organic framework (MOF) (Ln = Gd/Dy) by the slow release of oxalates in situ from organic ligands (disodium edetate dehydrate (EDTA-2Na) and thiodiglycolic acid).

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!